Medi-Plant Intl.
Country not established
- Devices
- 1
What Medi-Plant Intl. makes
Medi-Plant Intl. manufactures the Pour Bottle Decanter #2010, a Class II medical device designed for controlled liquid dispensing in clinical or procedural settings.
The company’s product is regulated under FDA 510(k) clearance as a Class II device and is listed in the U.S. regulatory database. The manufacturer operates from the United States.
Catalogue
Pour Bottle Decanter #2010 Ref K823538
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medi-Plant Intl. have in the registry?
The registry currently lists 1 device for Medi-Plant Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medi-Plant Intl.'s devices?
Among its 1 most recently registered device, Medi-Plant Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Medi-Plant Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medi-Plant Intl.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medi-Plant Intl. in the registry?
The most recently registered devices listed for Medi-Plant Intl. include POUR BOTTLE DECANTER #2010.